Evidence map›Paper›PMID 41700914›Full record

ArticleJCI insight2026

Reduced late endosome/lysosome function promotes SLE through chronic PI3K activity and SHP-1/SHIP-1 defects.

SunAh Kang, Andrew J Monteith, Liubov Arbeeva, Karissa Grier, Shruti Saxena Beem, Anthony C Trujillo, Xinyun Bi, Kai Sun, Rebecca E Sadun, Mithu Maheswaranathan and 4 more

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

SunAh KangDepartment of Microbiology and Immunology and.
Andrew J MonteithDepartment of Microbiology and Immunology and.
Liubov ArbeevaDivision of Rheumatology, Allergy, and Immunology, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Karissa GrierDivision of Rheumatology and Immunology, Duke University Medical Center, Durham, North Carolina, USA.
Shruti Saxena BeemDivision of Rheumatology, Allergy, and Immunology, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Anthony C TrujilloDivision of Rheumatology, Allergy, and Immunology, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Xinyun BiDepartment of Microbiology and Immunology and.
Kai SunDivision of Rheumatology and Immunology, Duke University Medical Center, Durham, North Carolina, USA.
Rebecca E SadunDivision of Rheumatology and Immunology, Duke University Medical Center, Durham, North Carolina, USA.
Mithu MaheswaranathanDivision of Rheumatology and Immunology, Duke University Medical Center, Durham, North Carolina, USA.
Megan Eb ClowseDivision of Rheumatology and Immunology, Duke University Medical Center, Durham, North Carolina, USA.
Saira Z SheikhDivision of Rheumatology, Allergy, and Immunology, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Jennifer L RogersDivision of Rheumatology and Immunology, Duke University Medical Center, Durham, North Carolina, USA.
Barbara J VilenDepartment of Microbiology and Immunology and.

Funding

UNC Core Center for Clinical ResearchP30AR072580 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LEIGH Fleming CALLAHAN, Amanda E Nelson · 2019 to 2026
$6.1M
NIAMS NIH HHS P30 AR072580
6 · The paper itself

Abstract

Degradation of cellular waste from phagocytosis, endocytosis, and autophagy occurs through hydrolases that become activated during acidification of late endosomes and lysosomes (LELs). In our cross-sectional study, we showed diminished LEL acidification and the accumulation of surface-bound nucleosome on monocytes, dendritic cells, B cells, neutrophils, and T cells from patients with systemic lupus erythematosus (SLE). Diminished acidification and exocytosis of undegraded IgG-immune complexes were evident in active, but not inactive, disease. This was supported by our murine study in which LEL acidification was diminished, promoting exocytosis and the accumulation of cell surface IgG-immune complexes. Mechanistically, LEL dysfunction was induced by chronic PI3K activation in lupus-prone MRL/lpr mice. We also showed that on a non-autoimmune C57BL/6 background, deficiency in SHP-1 and inhibition of SHIP-1 activity were sufficient to recapitulate LEL dysfunction found in MRL/lpr mice. Non-acidic LELs were evident in the majority of patients and associated with SLEDAI arthritis, rash, and nephritis. The high frequency of LEL dysfunction in SLE suggests that it could serve as a biomarker identifying a specific disease endotype.

Indexed as

EndosomesLupus Erythematosus, SystemicLysosomesPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphatidylinositol 3-KinasesProtein Tyrosine Phosphatase, Non-Receptor Type 6AnimalsDisease Models, AnimalFemaleHumansMiceMice, Inbred C57BLMice, Inbred MRL lprINPP5D protein, humanInpp5d protein, mousePhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphatidylinositol 3-KinasesProtein Tyrosine Phosphatase, Non-Receptor Type 6Ptpn6 protein, mouseAutoimmune diseasesAutoimmunityImmunologyLupusLysosomes

Identifiers

PMID41700914
PMCPMC13043080

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.